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    URINARY DRAINAGE BAG, (REORDER NO. 0749 - PRODUCT NO. 900-749)

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    P.F.C. SIGMA

    FDA UDI
    DEPUY (IRELAND)·10603295243687·P.F.C. SIGMA TIBIAL COMPONENT ALL POLY STABILIZ...

    Sklar

    FDA UDI
    SKLAR CORPORATION·50649111076358·KELLY FCP STR 5 1/2 INCHES STRL C100

    INNERSCAN BODY COMPOSITION MONITOR, INNERSCAN SEGMENTAL BODY COMPOSITION MONITOR

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    Smart Photon Micro-current Device, Model: EP-300

    FDA 510(k)
    FDA Class 2 ·Neurology

    PARADIGM REAL-TIME REVEL INSULIN INFUSION PUMP

    FDA Adverse Event
    Injury ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OYC·February 14, 2013

    SPRINT FIDELIS

    FDA Adverse Event
    Death ·MEDTRONIC PUERTO RICO, INC.·Product code LWS·January 18, 2011

    ACRYSOF RESTOR

    FDA Adverse Event
    Injury ·ALCON RESEARCH LTD/HUNTINGTON·Product code HQL·July 16, 2014

    Depuy P.F.C. E Knee System, stabilized all-polyethylene tibia, Sz 4, 12.5 mm; Ref 96-2652.

    FDA Recall
    Terminated ·Depuy Orthopaedics, Inc.·Product code NJL·May 26, 2005

    Depuy P.F.C. E Knee System Stabilized All-Polyethylene Tibia, 76mm M/L, 51mm A/P, 12.5mm, 4, UHMWPE, sterile; Product Code/REF 96-2652.

    FDA Recall
    Terminated ·Depuy Orthopaedics, Inc.·Product code NJL·September 27, 2007